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Wilson disease presents as a rare genetic disorder that results in an accumulation of copper in various organs. This progressive condition may impact the liver, brain, eyes, and other organs. Symptoms range widely can present as liver damage, neurological problems, and eye issues. Early diagnosis and treatment are essential in preventing the progre
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly discharge excess copper. Normally, the liver plays a crucial role in managing copper levels, moving it to other parts of the body where it is needed for various functions. However, in individuals with Wilson disease, mutations in the ATP7B gene disrupt this